A n1-((ethylimino)methylene)-n3,n3-dimethylpropane-1,3-diamine hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of n1-((ethylimino)methylene)-n3,n3-dimethylpropane-1,3-diamine hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of n1-((ethylimino)methylene)-n3,n3-dimethylpropane-1,3-diamine hydrochloride DMFs exist exist since differing nations have different regulations, such as n1-((ethylimino)methylene)-n3,n3-dimethylpropane-1,3-diamine hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A n1-((ethylimino)methylene)-n3,n3-dimethylpropane-1,3-diamine hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. n1-((ethylimino)methylene)-n3,n3-dimethylpropane-1,3-diamine hydrochloride USDMF includes data on n1-((ethylimino)methylene)-n3,n3-dimethylpropane-1,3-diamine hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The n1-((ethylimino)methylene)-n3,n3-dimethylpropane-1,3-diamine hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
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